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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 37221생성일: 2026년 10월 23일

Triethylamine → HCID 178441839, 화합물

https://huagongshe.com/ko/reaction/37221

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Valeryl chlorideHCID 61186—
반응물2-Amino-5-methylbenzoic acidHCID 76255—
반응물Ethyl acetate hexaneHCID 21226206—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
생성물HCID 178441839HCID 17844183925%

반응 조건

온도0 °C

반응 단계

To a solution of 3.0 g (20 mmol) of 2-amino-5-methyl benzoic acid in 20 mL of dry DMF at 0° C. was added 200 mg of DMAP followed by 6.07 g (60 mmol) of triethylamine and 5.02 g (40 mmol) of valeryl chloride. The resulting mixture was stirred at 0° C. for 30 min. The mixture was heated to 110° C. and monitored by TLC for the formation of the intermediate quinoxazolone (Rf =0.8, 40% EtOAc/hexane). Following complete formation of the intermediate 10 g (100 mmol) of (NH4)2CO3 was added cautiously. Heating was continued to ensure consumption of the quinoxazolone and formation of the polar (Rf =0.4, 40% EtOAc/hexane) quinazolin-4(1H)-one. The reaction mixture was concentrated in vacuo and the residue was taken up in 50 mL of ether and 50 mL of water. The mixture was filtered and the filtrate discarded after washing the residue with 20 mL of ether. The residue was recrystalized from MeOH to give 1.07 g (25%) of the title compound as a white crystalline solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05420133
출처 데이터셋uspto-grants-1995_05
ORD IDord-e9d62138891645b49a8ad36a194e69d0
출처 메모uspto-grants-1995_05